Apply and improve standard manufacturing approaches to ensure robust, capable production processes.

Support quality and regulatory compliance during product introduction, including coordination of process and equipment qualification activities.

Serve as a technical liaison with Quality to ensure requirements are met and documentation is complete and compliant.

Interface with Purchasing and suppliers to define and clarify incoming material technical requirements.

Develop, evaluate, and improve manufacturing methods to reduce lead time and increase yield.

Prepare technical analyses and project status updates for leadership review.

Analyze workforce utilization, space requirements, and workflow, and support equipment and workspace layout for optimal efficiency.

Experience in a FDA, ISO13485, or other highly regulated environment required.

Master’s degree in an Engineering or Science discipline from an accredited institution

Working knowledge of ERP systems (e.g., Visual, Oracle, SAP) and electronic Device History Record (eDHR) systems

Experience in medical device manufacturing, preferably ultrasound transducers

Experience with process risk evaluation and mitigation techniques, including pFMEA

Proficiency in data analysis, including statistical methods and visualization

Demonstrated project management skills

Demonstrates energy, ownership, and enthusiasm in day‑to‑day work